Canonical Allele Identifier: CA2709139586
Gene: CWC27 HGNC NCBI

Linked Data

dbSNP Id: rs2111806658
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.65051711G>A , CM000667.2:g.65051711G>A GRCh38
NC_000005.9:g.64347538G>A , CM000667.1:g.64347538G>A GRCh37
NC_000005.8:g.64383294G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693303.1:c.1153-47541G>A ENSP00000508557.1:n.1153-47541G>A
Search 100 bp 5'
Search 100 bp 3'